Your Trusted Partner for Clinical Trials in the Balkans
Delivering Excellence in Clinical Research with Over 20 Years of Local Expertise
Projects Done
Years of Experience
Satisfied Clients
Internal Expertise
Where Expertise Creates Excellence
With over 20 years of experience and deep knowledge of local regulations, we are the preferred partner for pharmaceutical and biotech companies conducting clinical trials in Serbia.
Our strong network of researchers and healthcare sites ensures the successful execution of your studies
Strategic Planning
Problem-Solving
01
Initial Consultation
02
Feasibility & Planning
03
Trial Execution
04
Final Delivery
Why Work With Us?
Whether you’re a clinical trial sponsor looking to expand into new markets or a CRO without a local presence in Serbia, EBS Clinical Research is here to be your trusted, local partner.
Serbia is a strategic choice for clinical trials, offering efficient regulatory pathways, experienced investigators, and access to a large pool of advanced therapy-naive patients.
If your CRO doesn’t currently operate in Serbia, that could limit your ability to include this rapidly growing market in your proposals. By partnering with EBS, you gain a reliable local ally who can seamlessly extend your reach and help position Serbia as a compelling trial destination for your clients.
In today’s clinical research landscape, strategic partnerships are key—and we’re here to help you deliver results with confidence and efficiency.
- Regulatory Expertise
- Patient-Centric Approach
- Accelerated Timelines
- Local Network Access
- Cost-Efficient Execution
- Full-Service CRO Solutions
Where Expertise Drives Breakthroughs
Study Startup Expertise:
Rapid site initiation with comprehensive feasibility assessments, ensuring your study starts on time and within scope.
Feasibility Services:
We use our deep local knowledge and strong relationships with investigators to deliver accurate, actionable insights that support your study planning.
Monitoring Excellence:
Ensuring the highest standards of data integrity and compliance through rigorous on-site and remote monitoring.
Let’s Accelerate Your Clinical Trial Together
We’re just a message away—let’s make things happen.
Ask. Explore. Execute.
Don’t see what you need? Just ask—we’re happy to help.
Partnering with a local CRO offers several key advantages for regional studies—including in-depth knowledge of the local regulatory landscape, strong relationships with investigators and clinical sites, and greater flexibility in operations.
Yes, we provide feasibility and site selection services, supported by deep local knowledge and an extensive network of trusted investigators and clinical sites across Serbia to ensure optimal site performance.
Yes, we’re highly adaptable to meet the specific needs of your study. We offer flexible operational models that can be tailored to your requirements, supported by proactive project management for quick decision-making. Our local teams work closely with your global teams to ensure everything runs smoothly.
Working with a local CRO often means significantly lower operational costs compared to large global CROs—without compromising on quality or performance. Because we operate on a more agile scale, we're able to offer cost-effective solutions while providing greater attention and dedication to each project. You get the expertise you need, along with personalized service and true partnership throughout your study.
condimentum, venenatis elementum.
Our team brings extensive experience and is skilled in managing clinical studies across a variety of therapeutic areas. We’re fully capable of working according to your specific SOPs while ensuring full compliance with all local regulatory requirements. This combination of adaptability and local expertise helps us deliver high-quality, compliant results tailored to your needs.
Yes, we provide feasibility and site selection services, supported by deep local knowledge and an extensive network of trusted investigators and clinical sites across Serbia to ensure optimal site performance.
We have extensive experience conducting a wide range of clinical trials, including medical device and IMP studies, as well as non-interventional, post-marketing, and observational studies. Our strongest expertise lies in managing Phase II–IV clinical trials across various therapeutic areas.
We’re highly flexible and able to adapt to each sponsor’s specific requirements and timelines. As an independent local CRO, we have the freedom to tailor our approach without rigid corporate constraints, allowing us to respond quickly and efficiently. Combined with our in-depth knowledge of local regulatory and operational requirements, this flexibility ensures timely execution aligned with your study goals.
Serbia is a highly strategic choice for clinical trials, offering a combination of efficient regulatory processes, experienced investigators, and access to a large pool of advanced therapy-naive patients. The healthcare infrastructure supports high-quality data collection, and patient recruitment is often faster due to strong interest in clinical research.